Correlation between the electronic structure and surface acidity of TiO2-SO
42- with different SO42- amounts has been investigated by means of NH3-TPD,
NH3-FT-IR and XPS. With the increase of sulfate loadings, the shift of bin
ding energies of O 1s in hydroxyl and Ti 2p(2/3) increases and is proportio
nal to total acidity. A linear relation is obtained between Ti 2p binding e
nergy shift and Lewis acid sites, while the shift in O 1s binding energy is
attributed both to the generation of NH3 hydrogen bond and of Bronsted aci
d sites. Accordingly, the results obtained from XPS measurements provide ev
idence that the ammonia adsorption sites are attributed to the decrease of
electron density of O 1s in hydroxyl (Bronsted type and H bonded) and Ti 2p
(2/3) (Lewis type) by inductive effect of the neighboring sulfate ion.